JPH0234943B2 - - Google Patents
Info
- Publication number
- JPH0234943B2 JPH0234943B2 JP56153404A JP15340481A JPH0234943B2 JP H0234943 B2 JPH0234943 B2 JP H0234943B2 JP 56153404 A JP56153404 A JP 56153404A JP 15340481 A JP15340481 A JP 15340481A JP H0234943 B2 JPH0234943 B2 JP H0234943B2
- Authority
- JP
- Japan
- Prior art keywords
- formula
- general formula
- represented
- imidazole derivative
- derivative according
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 150000002460 imidazoles Chemical class 0.000 claims description 23
- -1 1,3-disubstituted imidazole Chemical class 0.000 claims description 21
- 238000004519 manufacturing process Methods 0.000 claims description 19
- 125000004432 carbon atom Chemical group C* 0.000 claims description 14
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 7
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 4
- 125000004450 alkenylene group Chemical group 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
- 125000002252 acyl group Chemical group 0.000 claims 3
- 125000001931 aliphatic group Chemical group 0.000 claims 3
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims 1
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 37
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 24
- 238000006243 chemical reaction Methods 0.000 description 16
- 238000000034 method Methods 0.000 description 15
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 238000000862 absorption spectrum Methods 0.000 description 7
- 238000001914 filtration Methods 0.000 description 7
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 7
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N DMSO Substances CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 6
- 239000013078 crystal Substances 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 239000002994 raw material Substances 0.000 description 6
- VIHYIVKEECZGOU-UHFFFAOYSA-N N-acetylimidazole Chemical compound CC(=O)N1C=CN=C1 VIHYIVKEECZGOU-UHFFFAOYSA-N 0.000 description 5
- 238000000921 elemental analysis Methods 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- VWUCIBOKNZGWLX-UHFFFAOYSA-N 1h-imidazol-1-ium;bromide Chemical compound [Br-].C1=C[NH+]=CN1 VWUCIBOKNZGWLX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- MNWSURPQQVIQRL-UHFFFAOYSA-M [Br-].C1=CC(C=CC(=O)OC)=CC=C1CN1C=[N+](C(C)=O)C=C1 Chemical compound [Br-].C1=CC(C=CC(=O)OC)=CC=C1CN1C=[N+](C(C)=O)C=C1 MNWSURPQQVIQRL-UHFFFAOYSA-M 0.000 description 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
- KVNRLNFWIYMESJ-UHFFFAOYSA-N butyronitrile Chemical compound CCCC#N KVNRLNFWIYMESJ-UHFFFAOYSA-N 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 3
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 108010069102 Thromboxane-A synthase Proteins 0.000 description 2
- GANYMSDHMBJFIL-UHFFFAOYSA-N acetonitrile;ethoxyethane Chemical compound CC#N.CCOCC GANYMSDHMBJFIL-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- YICRPEGTQDSFEX-UHFFFAOYSA-N ethyl imidazole-1-carboxylate Chemical compound CCOC(=O)N1C=CN=C1 YICRPEGTQDSFEX-UHFFFAOYSA-N 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- ZSRCGGBALFGALF-UHFFFAOYSA-N methyl 3-[4-(bromomethyl)phenyl]prop-2-enoate Chemical compound COC(=O)C=CC1=CC=C(CBr)C=C1 ZSRCGGBALFGALF-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 229940124597 therapeutic agent Drugs 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RMDBHIHGJNGKDD-QPJJXVBHSA-N (e)-3-(2-methylphenyl)prop-2-enenitrile Chemical compound CC1=CC=CC=C1\C=C\C#N RMDBHIHGJNGKDD-QPJJXVBHSA-N 0.000 description 1
- QMICLBLOVTXNIY-ZZXKWVIFSA-N (e)-3-(3-methylphenyl)prop-2-enenitrile Chemical compound CC1=CC=CC(\C=C\C#N)=C1 QMICLBLOVTXNIY-ZZXKWVIFSA-N 0.000 description 1
- JBOIAZWJIACNJF-UHFFFAOYSA-N 1h-imidazole;hydroiodide Chemical compound [I-].[NH2+]1C=CN=C1 JBOIAZWJIACNJF-UHFFFAOYSA-N 0.000 description 1
- IYZRKPDDKSEWCW-UHFFFAOYSA-N 2-(2-bromoethyl)benzonitrile Chemical compound BrCCC1=CC=CC=C1C#N IYZRKPDDKSEWCW-UHFFFAOYSA-N 0.000 description 1
- MVIRKWKVTSPBQQ-UHFFFAOYSA-N 2-(4-cyanophenyl)ethyl 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)OCCC1=CC=C(C#N)C=C1 MVIRKWKVTSPBQQ-UHFFFAOYSA-N 0.000 description 1
- QGXNHCXKWFNKCG-UHFFFAOYSA-N 2-(bromomethyl)benzonitrile Chemical compound BrCC1=CC=CC=C1C#N QGXNHCXKWFNKCG-UHFFFAOYSA-N 0.000 description 1
- ZSHNOXOGXHXLAV-UHFFFAOYSA-N 2-(chloromethyl)benzonitrile Chemical compound ClCC1=CC=CC=C1C#N ZSHNOXOGXHXLAV-UHFFFAOYSA-N 0.000 description 1
- RJLJFDFQGDMDQP-UHFFFAOYSA-N 2-[4-(2-bromoethyl)phenyl]acetonitrile Chemical compound BrCCC1=CC=C(CC#N)C=C1 RJLJFDFQGDMDQP-UHFFFAOYSA-N 0.000 description 1
- JFTLITRZMNKVBD-UHFFFAOYSA-N 3-(2-bromoethyl)benzonitrile Chemical compound BrCCC1=CC=CC(C#N)=C1 JFTLITRZMNKVBD-UHFFFAOYSA-N 0.000 description 1
- SHCYJKVSXCAQAN-UHFFFAOYSA-N 3-(3-bromopropyl)benzonitrile Chemical compound BrCCCC1=CC=CC(C#N)=C1 SHCYJKVSXCAQAN-UHFFFAOYSA-N 0.000 description 1
- WIHQSUYGPGEXRW-UHFFFAOYSA-N 3-(4-cyanophenyl)propyl 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)OCCCC1=CC=C(C#N)C=C1 WIHQSUYGPGEXRW-UHFFFAOYSA-N 0.000 description 1
- CVKOOKPNCVYHNY-UHFFFAOYSA-N 3-(bromomethyl)benzonitrile Chemical compound BrCC1=CC=CC(C#N)=C1 CVKOOKPNCVYHNY-UHFFFAOYSA-N 0.000 description 1
- WRXVOTDGLNPNND-UHFFFAOYSA-N 3-(chloromethyl)benzonitrile Chemical compound ClCC1=CC=CC(C#N)=C1 WRXVOTDGLNPNND-UHFFFAOYSA-N 0.000 description 1
- BVGINDBNCSPHPC-UHFFFAOYSA-N 3-[4-(1h-imidazol-2-ylmethyl)phenyl]prop-2-enoic acid;hydrate;hydrochloride Chemical compound O.Cl.C1=CC(C=CC(=O)O)=CC=C1CC1=NC=CN1 BVGINDBNCSPHPC-UHFFFAOYSA-N 0.000 description 1
- MMSGPNSHDIKINF-UHFFFAOYSA-N 3-[4-(bromomethyl)phenyl]prop-2-enenitrile Chemical compound BrCC1=CC=C(C=CC#N)C=C1 MMSGPNSHDIKINF-UHFFFAOYSA-N 0.000 description 1
- NXMKGRQBJYESPD-UHFFFAOYSA-N 3-[4-(chloromethyl)phenyl]prop-2-enenitrile Chemical compound ClCC1=CC=C(C=CC#N)C=C1 NXMKGRQBJYESPD-UHFFFAOYSA-N 0.000 description 1
- UYQPFSLMGMVNPT-UHFFFAOYSA-N 3-benzyl-1H-imidazol-3-ium bromide Chemical compound [Br-].C(C1=CC=CC=C1)N1C=[NH+]C=C1 UYQPFSLMGMVNPT-UHFFFAOYSA-N 0.000 description 1
- NNNRGWOWXNCGCV-UHFFFAOYSA-N 4-(2-bromoethyl)benzonitrile Chemical compound BrCCC1=CC=C(C#N)C=C1 NNNRGWOWXNCGCV-UHFFFAOYSA-N 0.000 description 1
- PQBAYBHIVPRINR-UHFFFAOYSA-N 4-(2-iodoethyl)benzonitrile Chemical compound C1(=CC=C(C=C1)C#N)CCI PQBAYBHIVPRINR-UHFFFAOYSA-N 0.000 description 1
- CSDPTLGTZDYFHA-UHFFFAOYSA-N 4-(3-bromoprop-1-enyl)benzonitrile Chemical compound BrCC=CC1=CC=C(C#N)C=C1 CSDPTLGTZDYFHA-UHFFFAOYSA-N 0.000 description 1
- GSQHPAQTFSHMPZ-UHFFFAOYSA-N 4-(3-bromopropyl)benzonitrile Chemical compound BrCCCC1=CC=C(C#N)C=C1 GSQHPAQTFSHMPZ-UHFFFAOYSA-N 0.000 description 1
- KXTROGZCAWNOGO-UHFFFAOYSA-N 4-(3-iodoprop-1-enyl)benzonitrile Chemical compound ICC=CC1=CC=C(C#N)C=C1 KXTROGZCAWNOGO-UHFFFAOYSA-N 0.000 description 1
- ALERGPWUQNJOTK-UHFFFAOYSA-N 4-(3-iodopropyl)benzonitrile Chemical compound ICCCC1=CC=C(C#N)C=C1 ALERGPWUQNJOTK-UHFFFAOYSA-N 0.000 description 1
- UMLFTCYAQPPZER-UHFFFAOYSA-N 4-(bromomethyl)benzonitrile Chemical compound BrCC1=CC=C(C#N)C=C1 UMLFTCYAQPPZER-UHFFFAOYSA-N 0.000 description 1
- LOQLDQJTSMKBJU-UHFFFAOYSA-N 4-(chloromethyl)benzonitrile Chemical compound ClCC1=CC=C(C#N)C=C1 LOQLDQJTSMKBJU-UHFFFAOYSA-N 0.000 description 1
- XVCMLNJYQSBFPR-UHFFFAOYSA-N 4-(iodomethyl)benzonitrile Chemical compound ICC1=CC=C(C#N)C=C1 XVCMLNJYQSBFPR-UHFFFAOYSA-N 0.000 description 1
- MPSMSPGPJUQIBT-UHFFFAOYSA-N CC1=CC=C(C=C1)S(=O)(=O)OCCC1=CC=C(C=C1)CC#N Chemical compound CC1=CC=C(C=C1)S(=O)(=O)OCCC1=CC=C(C=C1)CC#N MPSMSPGPJUQIBT-UHFFFAOYSA-N 0.000 description 1
- GDBUORNHWAZSNU-UHFFFAOYSA-N N-propanoylimidazole Chemical compound CCC(=O)N1C=CN=C1 GDBUORNHWAZSNU-UHFFFAOYSA-N 0.000 description 1
- QOSMNYMQXIVWKY-UHFFFAOYSA-N Propyl levulinate Chemical compound CCCOC(=O)CCC(C)=O QOSMNYMQXIVWKY-UHFFFAOYSA-N 0.000 description 1
- RRBOJWNALRHFDE-UHFFFAOYSA-M [Br-].C1=[N+](C(=O)C)C=CN1CC1=CC=C(C=CC#N)C=C1 Chemical compound [Br-].C1=[N+](C(=O)C)C=CN1CC1=CC=C(C=CC#N)C=C1 RRBOJWNALRHFDE-UHFFFAOYSA-M 0.000 description 1
- QVLMMRHRZVZQCO-UHFFFAOYSA-M [Br-].CCOC(=O)C=CC1=CC=CC(CN2C=[N+](C=C2)C(C)=O)=C1 Chemical compound [Br-].CCOC(=O)C=CC1=CC=CC(CN2C=[N+](C=C2)C(C)=O)=C1 QVLMMRHRZVZQCO-UHFFFAOYSA-M 0.000 description 1
- BRNNSHAMFBHTTN-UHFFFAOYSA-M [Br-].CCOC(=O)C=CC1=CC=CC=C1CN1C=[N+](C(C)=O)C=C1 Chemical compound [Br-].CCOC(=O)C=CC1=CC=CC=C1CN1C=[N+](C(C)=O)C=C1 BRNNSHAMFBHTTN-UHFFFAOYSA-M 0.000 description 1
- CHNLRIPYLGFCTD-UHFFFAOYSA-M [I-].C1=CC(C=C(C)C(=O)OCC)=CC=C1CN1C=[N+](C(=O)C=2C=CC=CC=2)C=C1 Chemical compound [I-].C1=CC(C=C(C)C(=O)OCC)=CC=C1CN1C=[N+](C(=O)C=2C=CC=CC=2)C=C1 CHNLRIPYLGFCTD-UHFFFAOYSA-M 0.000 description 1
- BVJDLVOHTNKKAG-UHFFFAOYSA-M [I-].C1=CC(C=C(C)C(=O)OCC)=CC=C1CN1C=[N+](C(C)=O)C=C1 Chemical compound [I-].C1=CC(C=C(C)C(=O)OCC)=CC=C1CN1C=[N+](C(C)=O)C=C1 BVJDLVOHTNKKAG-UHFFFAOYSA-M 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- YFLFJABMYQGVCT-UHFFFAOYSA-M ethyl 3-[4-[(3-acetylimidazol-1-ium-1-yl)methyl]phenyl]propanoate;iodide Chemical compound [I-].C1=CC(CCC(=O)OCC)=CC=C1CN1C=[N+](C(C)=O)C=C1 YFLFJABMYQGVCT-UHFFFAOYSA-M 0.000 description 1
- LYOTVOZQURPWQB-UHFFFAOYSA-M ethyl 4-[3-(3-acetylimidazol-1-ium-1-yl)prop-1-enyl]benzoate;bromide Chemical compound [Br-].C1=CC(C(=O)OCC)=CC=C1C=CC[N+]1=CN(C(C)=O)C=C1 LYOTVOZQURPWQB-UHFFFAOYSA-M 0.000 description 1
- SKWYTDJNQHJYKR-UHFFFAOYSA-M ethyl 4-[3-(3-acetylimidazol-1-ium-1-yl)propyl]benzoate;iodide Chemical compound [I-].C1=CC(C(=O)OCC)=CC=C1CCCN1C=[N+](C(C)=O)C=C1 SKWYTDJNQHJYKR-UHFFFAOYSA-M 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N hydrochloric acid Substances Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- JEGIFBGJZPYMJS-UHFFFAOYSA-N imidazol-1-yl(phenyl)methanone Chemical compound C1=CN=CN1C(=O)C1=CC=CC=C1 JEGIFBGJZPYMJS-UHFFFAOYSA-N 0.000 description 1
- 150000004693 imidazolium salts Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- GIVCLXFKVGOEAT-UHFFFAOYSA-N methyl 2-(bromomethyl)-3-phenylprop-2-enoate Chemical compound COC(=O)C(CBr)=CC1=CC=CC=C1 GIVCLXFKVGOEAT-UHFFFAOYSA-N 0.000 description 1
- BUFDQKYCMATEEN-UHFFFAOYSA-N methyl 3-[4-(1h-imidazol-2-ylmethyl)phenyl]prop-2-enoate Chemical compound C1=CC(C=CC(=O)OC)=CC=C1CC1=NC=CN1 BUFDQKYCMATEEN-UHFFFAOYSA-N 0.000 description 1
- JTMONMQPMGOVPN-UHFFFAOYSA-M methyl 3-[4-[(3-benzoylimidazol-1-ium-1-yl)methyl]phenyl]prop-2-enoate;bromide Chemical compound [Br-].C1=CC(C=CC(=O)OC)=CC=C1CN1C=[N+](C(=O)C=2C=CC=CC=2)C=C1 JTMONMQPMGOVPN-UHFFFAOYSA-M 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- RZWIIPASKMUIAC-VQTJNVASSA-N thromboxane Chemical compound CCCCCCCC[C@H]1OCCC[C@@H]1CCCCCCC RZWIIPASKMUIAC-VQTJNVASSA-N 0.000 description 1
- DSNBHJFQCNUKMA-SCKDECHMSA-N thromboxane A2 Chemical compound OC(=O)CCC\C=C/C[C@@H]1[C@@H](/C=C/[C@@H](O)CCCCC)O[C@@H]2O[C@H]1C2 DSNBHJFQCNUKMA-SCKDECHMSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Priority Applications (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56153404A JPS5855466A (ja) | 1981-09-28 | 1981-09-28 | 新規な１，３−二置換イミダゾ−ル誘導体及びその製造方法 |
| US06/423,332 US4469865A (en) | 1981-09-28 | 1982-09-24 | 1,3-Disubstituted imidazoles |
| FI823291A FI823291L (fi) | 1981-09-28 | 1982-09-24 | Foerfarande foer produktion av 1,3-disubstituerade imidazoler |
| DK428382A DK428382A (da) | 1981-09-28 | 1982-09-27 | Hidtil ukendte 1,3-disubstituerede imidazoler og fremgangsmaade til deres fremstilling |
| HU823106A HU188808B (en) | 1981-09-28 | 1982-09-27 | Process for preparing 1,3-disubstituted imidazoles |
| CA000412356A CA1184185A (en) | 1981-09-28 | 1982-09-28 | 1,3-disubstituted imidazoles and a process for their production |
| ES516035A ES8308856A1 (es) | 1981-09-28 | 1982-09-28 | "un procedimiento para la produccion de un derivado de imidazol 1,3-disustituido". |
| KR1019820004368A KR840001558A (ko) | 1981-09-28 | 1982-09-28 | 1,3-디치환된 이미다졸의 제조방법 |
| EP82305099A EP0076140A3 (en) | 1981-09-28 | 1982-09-28 | 1,3-disubstituted imidazoles and a process for their production |
| AU88809/82A AU8880982A (en) | 1981-09-28 | 1982-09-28 | 1-acetyl(benzoyl)-3-(substituted benzyl)-imidazolium halides |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56153404A JPS5855466A (ja) | 1981-09-28 | 1981-09-28 | 新規な１，３−二置換イミダゾ−ル誘導体及びその製造方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5855466A JPS5855466A (ja) | 1983-04-01 |
| JPH0234943B2 true JPH0234943B2 (xx) | 1990-08-07 |
Family
ID=15561744
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56153404A Granted JPS5855466A (ja) | 1981-09-28 | 1981-09-28 | 新規な１，３−二置換イミダゾ−ル誘導体及びその製造方法 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US4469865A (xx) |
| EP (1) | EP0076140A3 (xx) |
| JP (1) | JPS5855466A (xx) |
| KR (1) | KR840001558A (xx) |
| AU (1) | AU8880982A (xx) |
| CA (1) | CA1184185A (xx) |
| DK (1) | DK428382A (xx) |
| ES (1) | ES8308856A1 (xx) |
| FI (1) | FI823291L (xx) |
| HU (1) | HU188808B (xx) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4581370A (en) * | 1983-07-12 | 1986-04-08 | Schering A.G. | Antiarrhythmic imidazoliums |
| CN103044333A (zh) * | 2013-01-11 | 2013-04-17 | 德州翰华医药化学有限公司 | 一种高纯度奥扎格雷钠的制备方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2643563A1 (de) * | 1976-09-28 | 1978-03-30 | Bayer Ag | Alpha-(4-biphenylyl)-benzyl-azolium- salze, verfahren zu ihrer herstellung sowie ihre verwendung zur bekaempfung von mikroorganismen |
| JPS55313A (en) * | 1978-06-13 | 1980-01-05 | Kissei Pharmaceut Co Ltd | Imidazole derivative |
| JPS56113766A (en) * | 1980-02-12 | 1981-09-07 | Teijin Ltd | Novel 1-substituted imidazole derivative and its preparation |
| JPS57131769A (en) * | 1981-02-10 | 1982-08-14 | Kissei Pharmaceut Co Ltd | 4-(1-imidazolylmethyl)cinnamic acid hydrochloride monohydrate, its preparation and drug containing the same |
-
1981
- 1981-09-28 JP JP56153404A patent/JPS5855466A/ja active Granted
-
1982
- 1982-09-24 FI FI823291A patent/FI823291L/fi not_active Application Discontinuation
- 1982-09-24 US US06/423,332 patent/US4469865A/en not_active Expired - Fee Related
- 1982-09-27 HU HU823106A patent/HU188808B/hu unknown
- 1982-09-27 DK DK428382A patent/DK428382A/da not_active Application Discontinuation
- 1982-09-28 ES ES516035A patent/ES8308856A1/es not_active Expired
- 1982-09-28 EP EP82305099A patent/EP0076140A3/en not_active Withdrawn
- 1982-09-28 AU AU88809/82A patent/AU8880982A/en not_active Abandoned
- 1982-09-28 KR KR1019820004368A patent/KR840001558A/ko unknown
- 1982-09-28 CA CA000412356A patent/CA1184185A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FI823291L (fi) | 1983-03-29 |
| AU8880982A (en) | 1983-04-14 |
| HU188808B (en) | 1986-05-28 |
| EP0076140A2 (en) | 1983-04-06 |
| ES516035A0 (es) | 1983-10-01 |
| US4469865A (en) | 1984-09-04 |
| ES8308856A1 (es) | 1983-10-01 |
| JPS5855466A (ja) | 1983-04-01 |
| FI823291A0 (fi) | 1982-09-24 |
| EP0076140A3 (en) | 1984-02-15 |
| DK428382A (da) | 1983-03-29 |
| KR840001558A (ko) | 1984-05-07 |
| CA1184185A (en) | 1985-03-19 |
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